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المؤلفون: Gisèle Bonne, Anne Bertrand, Carolina Epifano, Javier Ramón-Azcón, Alberto Martín, Albert G. Castaño, Miguel Ángel Rodríguez-Milla, Déborah Gómez-Domínguez, Fernando de Miguel, Borja Vilaplana-Martí, Sandra Amarilla-Quintana, Ignacio Pérez de Castro
المساهمون: Ministerio de Ciencia e Innovación (España), Instituto de Salud Carlos III, Instituto de Salud Carlos III [Madrid] (ISC), Universidad Europea de Madrid, Institute for Bioengineering of Catalonia [Barcelona] (IBEC), Institut de Myologie, Centre National de la Recherche Scientifique (CNRS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Association française contre les myopathies (AFM-Téléthon)-Sorbonne Université (SU), Centre de Recherche en Myologie, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Institució Catalana de Recerca i Estudis Avançats (ICREA), Centre de recherche en Myologie – U974 SU-INSERM
المصدر: Cells
Repisalud
Instituto de Salud Carlos III (ISCIII)
Cells, MDPI, 2020, 9 (5), pp.1286. ⟨10.3390/cells9051286⟩
Cells, Vol 9, Iss 1286, p 1286 (2020)
ABACUS. Repositorio de Producción Científica
Universidad Europea (UEM)
Volume 9
Issue 5مصطلحات موضوعية: life_sciences_other, 0301 basic medicine, Laminopathy, [SDV]Life Sciences [q-bio], Mutant, laminopathy, medicine.disease_cause, Muscle Development, LMNA, Myoblasts, Exon, Mice, 0302 clinical medicine, Tecnología médica, lcsh:QH301-705.5, Genetics, Mutation, integumentary system, Cell Differentiation, General Medicine, nuclear envelope, Exons, Lamin Type A, 030220 oncology & carcinogenesis, CRISPR, Female, C2C12, Microtubule-Associated Proteins, Subcellular Fractions, congenital, hereditary, and neonatal diseases and abnormalities, Cell Nucleus Shape, Membrana nuclear, Nuclear Envelope, MAP Kinase Signaling System, Telomere-Binding Proteins, Biology, Distrofias musculares, Article, Cell Line, 03 medical and health sciences, medicine, Animals, Protein kinase B, Cell Nucleus, Biología celular, Base Sequence, Membrane Proteins, medicine.disease, Genética, Clone Cells, 030104 developmental biology, lcsh:Biology (General), Lamin, DNA Damage
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ee86261be732949b99b100fed582abbTest
http://europepmc.org/articles/PMC7291140Test -
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المصدر: Cells, Vol 8, Iss 2, p 88 (2019)
Cellsمصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Laminopathy, miR9, Review, laminopathy, Biology, Bioinformatics, medicine.disease_cause, LMNA, Exon, Progeria, medicine, Animals, Humans, Genetic Predisposition to Disease, Gene, lcsh:QH301-705.5, lamin A/C, Mutation, integumentary system, nutritional and metabolic diseases, General Medicine, Genetic Therapy, medicine.disease, Progerin, gene therapy, Disease Models, Animal, Phenotype, lcsh:Biology (General), progerin, HGPS, Lamin
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de1c2aba3f250468fee31d74bb3d3199Test
https://www.mdpi.com/2073-4409/8/2/88Test